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An extremely rare case of Rosai-Dorfman disease in the spleen
BACKGROUND: Rosai-Dorfman disease (RDD) is a rare, multisystemic histiocytic disorder, and commonly manifesting as lymphadenopathy in the young male. Abdominal manifestations of RDD are extremely rare. CASE PRESENTATION: In August 2018, a 42-year-old man underwent an abdominal ultrasonography examin...
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| Publicado no: | BMC Surg |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7789675/ https://ncbi.nlm.nih.gov/pubmed/33407333 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12893-020-01014-0 |
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